52713000: Infantile neuroaxonal dystrophy (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy
\Central nervous system finding\Disorder of the central nervous system\Spastic syndrome\Infantile neuroaxonal dystrophy
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Degenerative brain disorder\...

\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy

\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy

\Disorder of head\Disorder of brain\Degenerative brain disorder\...

\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy

\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy

\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Spastic syndrome\Infantile neuroaxonal dystrophy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy
\Disease\Disorder of head\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Cerebral degeneration in childhood\Infantile neuroaxonal dystrophy
\Disease\Disorder of head\Disorder of brain\Degenerative brain disorder\Neuroaxonal dystrophy\Infantile neuroaxonal dystrophy

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

87716013 Infantile neuroaxonal dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

87717016 Seitelberger's disease en Synonym Active Entire term case sensitive SNOMED CT core module

87718014 Spastic amaurotic axonal idiocy en Synonym Active Entire term case insensitive SNOMED CT core module

790753012 Infantile neuroaxonal dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1231146019 Seitelberger disease en Synonym Active Entire term case insensitive SNOMED CT core module

1231147011 INAD - Infantile neuroaxonal dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Infantile neuroaxonal dystrophy	Is a	Spastic syndrome	false	Inferred relationship	Existential restriction modifier
Infantile neuroaxonal dystrophy	Is a	Cerebral degeneration in childhood	true	Inferred relationship	Existential restriction modifier
Infantile neuroaxonal dystrophy	Is a	Neuroaxonal dystrophy	true	Inferred relationship	Existential restriction modifier
Infantile neuroaxonal dystrophy	Associated morphology	Degeneration	false	Inferred relationship	Existential restriction modifier	1
Infantile neuroaxonal dystrophy	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	2
Infantile neuroaxonal dystrophy	Finding site	Structure of telencephalon	false	Inferred relationship	Existential restriction modifier
Infantile neuroaxonal dystrophy	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier	1
Infantile neuroaxonal dystrophy	Occurrence	Childhood	true	Inferred relationship	Existential restriction modifier	2
Infantile neuroaxonal dystrophy	Is a	Spastic syndrome	true	Inferred relationship	Existential restriction modifier
Infantile neuroaxonal dystrophy	Finding site	Structure of cerebrum	false	Inferred relationship	Existential restriction modifier	1
Infantile neuroaxonal dystrophy	Associated morphology	Degeneration	false	Inferred relationship	Existential restriction modifier	1
Infantile neuroaxonal dystrophy	Finding site	Structure of cerebrum	true	Inferred relationship	Existential restriction modifier	1
Infantile neuroaxonal dystrophy	Associated morphology	Degenerative abnormality	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
87716013	Infantile neuroaxonal dystrophy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
87717016	Seitelberger's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
87718014	Spastic amaurotic axonal idiocy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
790753012	Infantile neuroaxonal dystrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1231146019	Seitelberger disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1231147011	INAD - Infantile neuroaxonal dystrophy	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module